28 positions on this site are linked to Ovarian Cancer, out of 107,852 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.
LINC01111 · rs150293538
See detailed info → SensitivePVT1 · rs7833298
See detailed info → Sensitivenear BNC2 · rs10810671
See detailed info → SensitiveLINC02652 · rs1934363
See detailed info → SensitivePLEKHM1 · rs71238846
See detailed info → SensitiveGAL3ST2 · rs73011950
See detailed info → SensitiveADAM29 · rs6826366
See detailed info → SensitiveSTXBP4 · rs244353
See detailed info → SensitiveMSLNL · rs114590746
See detailed info → SensitiveGAL3ST2 · rs62193063
See detailed info → Sensitivenear TOMM5P1 · rs7748275
See detailed info → SensitiveESR1 · rs851980
See detailed info → SensitiveABHD8 · rs4808616
See detailed info → SensitiveLINC00824 · rs1400482
See detailed info → Sensitivenear FST · rs528577783
See detailed info → SensitiveGCLC · rs1013698558
See detailed info → SensitivePTPRD · rs768719522
See detailed info → SensitiveACD · rs6979
See detailed info → Sensitivenear MYC · rs9886651
See detailed info → Sensitivenear STN1 · rs7902587
See detailed info →Showing 20 of 28 · page 1 of 2
One specific position in the genome (an rsID), explained in plain language with what published research has found it linked to, and how strong that link actually is.
The public GWAS Catalog, checked every twenty minutes, plus variants added manually after research review. Every one passes the same quality gate before publishing.
No. Listing reflects an association from published research, not a diagnosis or a cause. Most common variants shift probability modestly rather than determining an outcome.
Yes — the search box above matches gene symbols and rsIDs as well as trait names.